Macular Sensitivity and Fixation Patterns in Patients with Autosomal Dominant Optic Atrophy

被引:0
|
作者
Ronnback, Cecilia [1 ,2 ]
Larsen, Michael [1 ,2 ]
机构
[1] Glostrup Cty Hosp, Dept Ophthalmol, Copenhagen, Denmark
[2] Univ Copenhagen, Fac Hlth Sci, Copenhagen, Denmark
关键词
613 neuro-ophthalmology: optic nerve; 758 visual fields;
D O I
暂无
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
6211
引用
收藏
页数:2
相关论文
共 50 条
  • [31] Genomic rearrangements in OPA1 are frequent in patients with autosomal dominant optic atrophy
    Fuhrmann, N.
    Alavi, M. V.
    Bitoun, P.
    Woernle, S.
    Auburger, G.
    Leo-Kottler, B.
    Yu-Wai-Man, P.
    Chinnery, P.
    Wissinger, B.
    JOURNAL OF MEDICAL GENETICS, 2009, 46 (02) : 136 - 144
  • [32] Genomic deletions in OPA1 in Danish patients with autosomal dominant optic atrophy
    Almind, Gitte J.
    Gronskov, Karen
    Milea, Dan
    Larsen, Michael
    Brondum-Nielsen, Karen
    Ek, Jakob
    BMC MEDICAL GENETICS, 2011, 12
  • [33] FALCON: A Prospective Natural History Study of Patients with Autosomal Dominant Optic Atrophy (ADOA)
    Gross, Steven
    Liao, Yaping Joyce
    Yu-Wai-Man, Patrick
    Lam, Byron L.
    Mudumbai, Raghu
    Votruba, Marcela
    Saluti, Kelly
    Wang, Yuw
    Ticho, Barry
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2024, 65 (07)
  • [34] Autosomal dominant optic atrophy:: Penetrance and expressivity in patients with OPA1 mutations
    Cohn, Amn C.
    Toomes, Carmel
    Potter, Catherine
    Towns, Katherine V.
    Hewitt, Alex W.
    Inglehearn, Chris F.
    Craig, Jamie E.
    Mackey, David A.
    AMERICAN JOURNAL OF OPHTHALMOLOGY, 2007, 143 (04) : 656 - 662
  • [35] OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritance
    Pesch, UEA
    Leo-Kottler, B
    Mayor, S
    Jurklies, B
    Kellner, U
    Apfelstedt-Sylla, E
    Zrenner, E
    Alexander, C
    Wissinger, B
    HUMAN MOLECULAR GENETICS, 2001, 10 (13) : 1359 - 1368
  • [36] Peripapillary and macular morpho-vascular changes in patients with genetic or clinical diagnosis of autosomal dominant optic atrophy: a case-control study
    Amélia Martins
    Tiago M. Rodrigues
    Mário Soares
    Michael-John Dolan
    Joaquim N. Murta
    Rufino Silva
    João P. Marques
    Graefe's Archive for Clinical and Experimental Ophthalmology, 2019, 257 : 1019 - 1027
  • [37] Peripapillary and macular morpho-vascular changes in patients with genetic or clinical diagnosis of autosomal dominant optic atrophy: a case-control study
    Martins, Amelia
    Rodrigues, Tiago M.
    Soares, Mario
    Dolan, Michael-John
    Murta, Joaquim N.
    Silva, Rufino
    Marques, Joao P.
    GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 2019, 257 (05) : 1019 - 1027
  • [38] Retinal vessel diameters decrease with macular ganglion cell layer thickness in autosomal dominant optic atrophy and in healthy subjects
    Ronnback, Cecilia
    Gronskov, Karen
    Larsen, Michael
    ACTA OPHTHALMOLOGICA, 2014, 92 (07) : 670 - 674
  • [39] Correlation between quality of vision and clinical and structural parameters in patients with Autosomal Dominant Optic Atrophy
    Camos-Carreras, Anna
    Figueras-Roca, Marc
    Alba-Arbalat, Salut
    Alcubierre, Rafel
    Saint-Gerons, Marta
    Sanchez-Dalmau, Bernardo
    EYE, 2025,
  • [40] OPA1 mutations in Japanese patients suspected to have autosomal dominant optic atrophy
    Tetsuya Hamahata
    Takuro Fujimaki
    Keiko Fujiki
    Ai Miyazaki
    Atsushi Mizota
    Akira Murakami
    Japanese Journal of Ophthalmology, 2012, 56 : 91 - 97